Fig. 7From: PARIS induced defects in mitochondrial biogenesis drive dopamine neuron loss under conditions of parkin or PINK1 deficiencyDopaminergic knockdown of Drosophila PARIS rescues dopaminergic neurotoxicity associated with reduced parkin or PINK1 activity. a Immunoblot analysis and quantification of dPARIS protein levels in flies expressing the indicated transgenes under the control of TH-Gal4 driver. b Dopaminergic knockdown of dPARIS promotes DA neuron survival under conditions of parkin or PINK1 knockdown in 30-day old flies. N = 10 flies per genotype. c Climbing defects associated with dopaminergic knockdown of parkin or PINK1 restored by dPARIS knockdown in DA neurons. N = 60 flies per indicated genotype. TH-Gal4/+ flies served as control. d Quantitative RT-PCR analysis of Drosophila homologs of PGC-1α (Spargel), NRF1 (ewg), NRF-2 (Delg) and mitochondrial transcriptional factor A (TFAM) in 30-day old fly heads from the indicated genotypes, N = 3. Quantitative data = mean ± SEM. One-way ANOVA *p < 0.05, **p < 0.01, *** p < 0.001, ****p < 0.0001. See also Additional file 16, Figure S6Back to article page